Pulmonary lymphangioleiomyomatosis Imaging Diagnosis_0.docVIP

 PAGE \* MERGEFORMAT 10 Pulmonary lymphangioleiomyomatosis Imaging Diagnosis [Abstract] Objective To investigate the pulmonary lymphangioleiomyomatosis imaging features to improve the diagnosis of the disease. Methods A retrospective analysis of our hospital diagnosed pulmonary lymphangioleiomyomatosis in 11 cases, all patients underwent chest X-ray examination and chest HRCT examination. The results show no obvious chest X-specific. HRCT features of diffuse lung showed round or polygonal cysts, cysts of about 2-40mm in diameter, most less than 10mm, wall thickness of small at 1mm. Conclusions Pulmonary lymphangioleiomyomatosis is a rare disease, which has characteristic imaging findings, especially HRCT imaging examination in the diagnosis of great significance. [Keywords:] Pulmonary lymphangioleiomyomatosis; tomography camera [Abstract] Objective to investigate image features of pulmonary lymphangioleiomyomatosis (PLAM) and to improve its diagnosis. Methods eleven patients with pathologically proved PLAM underwent chest X-ray and high resolution thoracic CT scanning, The clinical data and image features were retrospectively analyzed.Results The chest X-ray shows no characteristic manifestation, the characteristic HRCT manifestation was multiple, different sized cystoid transparent areas, which were diffusely distributed throughout both lungs. Most cysts were less than 10mm in diameter (2-40mm), the cysts cliff were less then 1mm. Conclusion PLAM is a rare disease, image examinations have characteristic signs especially HRCT [Keywords:] Pulmonary lymphangioleiomyomatosis; Tomography, X-ray computed; High resolution CT Pulmonary lymphangioleiomyomatosis (pulmonary lymphangioleiomyomatosis is a rare, cause unknown, the continued development of interstitial lung disease, mainly in women of childbearing age. Our hospital were diagnosed in 11 cases over the past decade, is to be reported, and on its imaging characteristics and chest with HRCT diagnos